Aims and background: Multiple endocrine neoplasia (MEN) syndromes include a
group of disorders characterized by the neoplastic transformation of two o
r more endocrine tissues. In type 1 syndrome (MEN-1), pituitary, parathyroi
d and pancreatic islet tumors are most frequently represented. Thymic neopl
asms are also rarely associated, and thymectomy during subtotal or total pa
rathyroidectomy should always be considered.
Study design: The authors describe a rare case of a 22-year-old male who pr
esented a type B1 thymoma without myasthenia gravis associated to hyperpara
thyroidism, corticoadrenal adenoma and three neuroendocrine pancreatic lesi
ons (somatostatinoma, glucagonoma and insulinoma).